As many of you know, Edie was diagnosed with Lupus in the spring of 2021. After several years of watching her suffer from bizarre and debilitating symptoms she has embraced a new way of life despite what I call the invisible monster. The fatigue, joint pain, rashes and mouth ulcers among some of the symptoms are always lurking and we never know when its going to rear its ugly head. We are committed to supporting education,research and advocacy to help others just like Edie. We are joining thousands of people across the country for the Walk to End Lupus Now®. I hope that you will join me either by lacing up your sneakers or by donating to my fundraising page.
Did you know?
Lupus is a mysterious and misunderstood autoimmune disease. It strikes without warning, affects each person differently, and has no known causes or cure.
Lupus symptoms can be severe and highly unpredictable and can damage any organ or tissue, from the skin or joints to the heart or kidneys.
Lupus is hard to diagnose, but the Lupus Foundation of America is working to make life easier and more comfortable for the estimated 1.5 million people living with lupus in the United States. Together, we can solve the cruel mystery of lupus. Thank you for your generosity!
